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PLX7904是有效的选择性悖论突破性RAF抑制剂。它能够有效抑制突变型BRAF黑色素瘤细胞中ERK1/2的激活,但不能过度激活突变型RAS表达细胞中的ERK1/2。
靶点信息
Raf | ||||
In vitro | DMSO | 87 mg/mL (169.75 mM) | |
Water | Insoluble | ||
Ethanol | Insoluble | ||
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
0.1 mM | 19.51 mL | 97.56 mL | 195.11 mL |
0.5 mM | 3.9 mL | 19.51 mL | 39.02 mL |
1 mM | 1.95 mL | 9.76 mL | 19.51 mL |
5 mM | 0.39 mL | 1.95 mL | 3.9 mL |
*The above data is based on the productmolecular weight 512.53. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
目录号 | A15855 |
---|---|
作用机制 | Inhibitor (抑制剂) |
M. Wt | 512.53 |
Formula | C24H22F2N6O3S |
Purity | >99% |
Storage | Store lyophilized at -20ºC, keep desiccated. |
CAS No. | 1393465-84-3 |
Synonyms | PB04 |
SMILES | O=C(C1=CNC2=NC=C(C3=CN=C(C4CC4)N=C3)C=C21)C5=C(F)C=CC(NS(=O)(N(CC)C)=O)=C5F |
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